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Eric D. Marsh, MD, PhD - Publications

Affiliations: 
Cell and Molecular Biology University of Pennsylvania, Philadelphia, PA, United States 
Area:
Human Development, Neuroscience Biology, Child Neurology
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77 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Hong W, Haviland I, Pestana-Knight E, Weisenberg JL, Demarest S, Marsh ED, Olson HE. CDKL5 Deficiency Disorder-Related Epilepsy: A Review of Current and Emerging Treatment. Cns Drugs. PMID 35633486 DOI: 10.1007/s40263-022-00921-5  0.345
2022 Kane O, McCoy A, Jada R, Borisov V, Zag L, Zag A, Schragenheim-Rozales K, Shalgi R, Levy NS, Levy AP, Marsh ED. Characterization of spontaneous seizures and EEG abnormalities in a mouse model of the human A350V IQSEC2 mutation and identification of a possible target for precision medicine based therapy. Epilepsy Research. 182: 106907. PMID 35344748 DOI: 10.1016/j.eplepsyres.2022.106907  0.383
2021 Joseph DJ, Von Deimling M, Hasegawa Y, Cristancho AG, Risbud R, McCoy AJ, Marsh ED. Protocol for isolating young adult parvalbumin interneurons from the mouse brain for extraction of high-quality RNA. Star Protocols. 2: 100714. PMID 34401780 DOI: 10.1016/j.xpro.2021.100714  0.456
2021 Siddiqi F, Trakimas AL, Joseph DJ, Lippincott ML, Marsh ED, Wolfe JH. Islet1 Precursors Contribute to Mature Interneuron Subtypes in Mouse Neocortex. Cerebral Cortex (New York, N.Y. : 1991). PMID 34228108 DOI: 10.1093/cercor/bhab152  0.478
2021 Joseph DJ, Von Deimling M, Hasegawa Y, Cristancho AG, Ahrens-Nicklas RC, Rogers SL, Risbud R, McCoy AJ, Marsh ED. Postnatal transcriptional activity regulates functional properties of PV interneurons. Iscience. 24: 101999. PMID 33490907 DOI: 10.1016/j.isci.2020.101999  0.708
2020 Terzic B, Cui Y, Edmondson AC, Tang S, Sarmiento N, Zaitseva D, Marsh ED, Coulter DA, Zhou Z. X-linked cellular mosaicism underlies age-dependent occurrence of seizure-like events in mouse models of CDKL5 deficiency disorder. Neurobiology of Disease. 105176. PMID 33197557 DOI: 10.1016/j.nbd.2020.105176  0.358
2020 Berecki G, Helbig KL, Ware TL, Grinton B, Skraban CM, Marsh ED, Berkovic SF, Petrou S. Novel Missense Mutations Associated with Infantile-Onset Developmental and Epileptic Encephalopathy. International Journal of Molecular Sciences. 21. PMID 32878331 DOI: 10.3390/Ijms21176333  0.374
2020 Shi X, Lim Y, Myers AK, Stallings BL, Mccoy A, Zeiger J, Scheck J, Cho G, Marsh ED, Mirzaa GM, Tao T, Golden JA. PIK3R2/Pik3r2 activating mutations result in brain overgrowth and EEG changes. Annals of Neurology. PMID 32856318 DOI: 10.1002/Ana.25890  0.318
2020 Mulcahey PJ, Tang S, Takano H, White A, Davila Portillo DR, Kane OM, Marsh ED, Zhou Z, Coulter DA. Aged heterozygous Cdkl5 mutant mice exhibit spontaneous epileptic spasms. Experimental Neurology. 113388. PMID 32585155 DOI: 10.1016/J.Expneurol.2020.113388  0.474
2020 Saby JN, Peters SU, Roberts TPL, Nelson CA, Marsh ED. Evoked Potentials and EEG Analysis in Rett Syndrome and Related Developmental Encephalopathies: Towards a Biomarker for Translational Research. Frontiers in Integrative Neuroscience. 14: 30. PMID 32547374 DOI: 10.3389/Fnint.2020.00030  0.324
2020 Chang BS, Krishnan V, Dulla CG, Jette N, Marsh ED, Dacks PA, Whittemore V, Poduri A. Epilepsy Benchmarks Area I: Understanding the Causes of the Epilepsies and Epilepsy-Related Neurologic, Psychiatric, and Somatic Conditions. Epilepsy Currents. 1535759719895280. PMID 31965828 DOI: 10.1177/1535759719895280  0.331
2019 Conrad EC, Tomlinson SB, Wong JN, Oechsel KF, Shinohara RT, Litt B, Davis KA, Marsh ED. Spatial distribution of interictal spikes fluctuates over time and localizes seizure onset. Brain : a Journal of Neurology. PMID 31860064 DOI: 10.1093/Brain/Awz386  0.374
2019 Gourmaud S, Shou H, Irwin DJ, Sansalone K, Jacobs LM, Lucas TH, Marsh ED, Davis KA, Jensen FE, Talos DM. Alzheimer-like amyloid and tau alterations associated with cognitive deficit in temporal lobe epilepsy. Brain : a Journal of Neurology. PMID 31834353 DOI: 10.1093/Brain/Awz381  0.348
2019 Ahrens-Nicklas RC, Tecedor L, Hall A, Lysenko E, Cohen AS, Davidson BL, Marsh ED. Neuronal network dysfunction precedes storage and neurodegeneration in a lysosomal storage disorder. Jci Insight. PMID 31573978 DOI: 10.1172/Jci.Insight.131961  0.339
2019 Gofshteyn JS, Le T, Kessler S, Kamens R, Carr C, Gaetz W, Bloy L, Roberts TPL, Schwartz ES, Marsh ED. Synthetic aperture magnetometry and excess kurtosis mapping of Magnetoencephalography (MEG) is predictive of epilepsy surgical outcome in a large pediatric cohort. Epilepsy Research. 155: 106151. PMID 31247475 DOI: 10.1016/J.Eplepsyres.2019.106151  0.375
2019 Tang S, Terzic B, Wang IJ, Sarmiento N, Sizov K, Cui Y, Takano H, Marsh ED, Zhou Z, Coulter DA. Altered NMDAR signaling underlies autistic-like features in mouse models of CDKL5 deficiency disorder. Nature Communications. 10: 2655. PMID 31201320 DOI: 10.1038/S41467-019-10689-W  0.361
2019 Demarest S, Pestana-Knight EM, Olson HE, Downs J, Marsh ED, Kaufmann WE, Partridge CA, Leonard H, Gwadry-Sridhar F, Frame KE, Cross JH, Chin RFM, Parikh S, Panzer A, Weisenberg J, et al. Severity Assessment in CDKL5 Deficiency Disorder. Pediatric Neurology. PMID 31147226 DOI: 10.1016/J.Pediatrneurol.2019.03.017  0.384
2019 Laux LC, Bebin EM, Checketts D, Chez M, Flamini R, Marsh ED, Miller I, Nichol K, Park Y, Segal E, Seltzer L, Szaflarski JP, Thiele EA, Weinstock A. Long-term safety and efficacy of cannabidiol in children and adults with treatmentresistant Lennox-Gastaut syndrome or Dravet syndrome: Expanded access program results. Epilepsy Research. 154: 13-20. PMID 31022635 DOI: 10.1016/J.Eplepsyres.2019.03.015  0.303
2019 Tomlinson SB, Wong JN, Conrad EC, Kennedy BC, Marsh ED. Reproducibility of interictal spike propagation in children with refractory epilepsy. Epilepsia. PMID 31006860 DOI: 10.1111/Epi.14720  0.381
2019 Billakota S, Devinsky O, Marsh E. Cannabinoid therapy in epilepsy Current Opinion in Neurology. 32: 220-226. PMID 30676535 DOI: 10.1097/Wco.0000000000000660  0.333
2019 Marsh E, Uchino K, Baker R. Cranial Efferent Neurons Extend Processes Through the Floor Plate in the Developing Hindbrain. The Biological Bulletin. 183: 354-356. PMID 29300641 DOI: 10.1086/Bblv183N2P354  0.4
2018 Neul JL, Benke TA, Marsh ED, Skinner SA, Merritt J, Lieberman DN, Standridge S, Feyma T, Heydemann P, Peters S, Ryther R, Jones M, Suter B, Kaufmann WE, Glaze DG, et al. The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 30536762 DOI: 10.1002/Ajmg.B.32707  0.319
2018 Rogers SL, Rankin-Gee E, Risbud RM, Porter BE, Marsh ED. Normal development of the Perineuronal net in humans; in patients with and without epilepsy. Neuroscience. PMID 29885523 DOI: 10.1016/J.Neuroscience.2018.05.039  0.69
2018 Tomlinson SB, Khambhati AN, Bermudez C, Kamens RM, Heuer GG, Porter BE, Marsh ED. Alterations of network synchrony after epileptic seizures: An analysis of post-ictal intracranial recordings in pediatric epilepsy patients. Epilepsy Research. 143: 41-49. PMID 29655171 DOI: 10.1016/J.Eplepsyres.2018.04.003  0.444
2018 Thiele EA, Marsh ED, French JA, Mazurkiewicz-Beldzinska M, Benbadis SR, Joshi C, Lyons PD, Taylor A, Roberts C, Sommerville K. Cannabidiol in patients with seizures associated with Lennox-Gastaut syndrome (GWPCARE4): a randomised, double-blind, placebo-controlled phase 3 trial. Lancet (London, England). PMID 29395273 DOI: 10.1016/S0140-6736(18)30136-3  0.392
2018 Hagopian SJ, Marsh ED. Cannabidiol for epilepsy: a new indication for an old drug Future Neurology. 13: 181-190. DOI: 10.2217/Fnl-2018-0022  0.328
2018 Tomlinson S, Khambhati A, Kamens RM, Porter BE, Marsh ED. 126 Postictal EEG Activity in Pediatric and Adult Patients Undergoing Epilepsy Surgery: A Network Perspective Neurosurgery. 65: 89-89. DOI: 10.1093/Neuros/Nyy303.126  0.353
2018 Marsh ED, Bergqvist AGC, Medne L, Hassoun P, Gonatas NK, Eagle RC, Viaene AN, Rorke-Adams LB. Novel Neuropathological Features of a Child with an Epileptic Encephalopathy Due to Presumed Polyol Dysmetabolism Journal of Pediatric Epilepsy. 7: 142-147. DOI: 10.1055/S-0039-1678560  0.325
2018 Tomlinson SB, Marsh ED. Simulating Neocortical Resections before Epilepsy Surgery: A Study of Intracranial Electroencephalography Recordings Journal of the American College of Surgeons. 227: S188. DOI: 10.1016/J.Jamcollsurg.2018.07.405  0.336
2018 Armstrong D, Marsh E. Cannabidiol in Pediatric Epilepsy Current Pediatrics Reports. 6: 26-29. DOI: 10.1007/S40124-018-0152-0  0.42
2017 Lee BH, Reijnders MRF, Abubakare O, Tuttle E, Lape B, Minks KQ, Stodgell C, Bennetto L, Kwon J, Fong CT, Gripp KW, Marsh ED, Smith WE, Huq AM, Coury SA, et al. Expanding the neurodevelopmental phenotype of PURA syndrome. American Journal of Medical Genetics. Part A. PMID 29150892 DOI: 10.1002/Ajmg.A.38521  0.364
2017 Masnada S, Hedrich UBS, Gardella E, Schubert J, Kaiwar C, Klee EW, Lanpher BC, Gavrilova RH, Synofzik M, Bast T, Gorman K, King MD, Allen NM, Conroy J, Ben Zeev B, ... ... Marsh E, et al. Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies. Brain : a Journal of Neurology. 140: 2337-2354. PMID 29050392 DOI: 10.1093/Brain/Awx184  0.401
2017 Helbig I, von Deimling M, Marsh ED. Epileptic Encephalopathies as Neurodegenerative Disorders. Advances in Neurobiology. 15: 295-315. PMID 28674986 DOI: 10.1007/978-3-319-57193-5_11  0.454
2017 Devinsky O, Cross JH, Laux L, Marsh E, Miller I, Nabbout R, Scheffer IE, Thiele EA, Wright S. Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome. The New England Journal of Medicine. 376: 2011-2020. PMID 28538134 DOI: 10.1056/Nejmoa1611618  0.391
2017 Zou F, McWalter K, Schmidt L, Decker A, Picker JD, Lincoln S, Sweetser DA, Briere LC, Harini C, Marsh E, Medne L, Wang RY, Leydiker K, Mower A, et al. Expanding the phenotypic spectrum of GABRG2 variants: a recurrent GABRG2 missense variant associated with a severe phenotype. Journal of Neurogenetics. 1-7. PMID 28460589 DOI: 10.1080/01677063.2017.1315417  0.433
2017 von Deimling M, Helbig I, Marsh ED. Epileptic Encephalopathies-Clinical Syndromes and Pathophysiological Concepts. Current Neurology and Neuroscience Reports. 17: 10. PMID 28229394 DOI: 10.1007/S11910-017-0720-7  0.443
2017 Tomlinson SB, Porter BE, Marsh ED. Interictal network synchrony and local heterogeneity predict epilepsy surgery outcome among pediatric patients. Epilepsia. PMID 28166392 DOI: 10.1111/Epi.13657  0.398
2017 Olson HE, Kelly M, LaCoursiere CM, Pinsky R, Tambunan D, Shain C, Ramgopal S, Takeoka M, Libenson MH, Julich K, Loddenkemper T, Marsh ED, Segal D, Koh S, Salman MS, et al. Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression. Annals of Neurology. PMID 28133863 DOI: 10.1002/Ana.24883  0.344
2017 Gofshteyn JS, Wilfong A, Devinsky O, Bluvstein J, Charuta J, Ciliberto MA, Laux L, Marsh ED. Cannabidiol as a Potential Treatment for Febrile Infection-Related Epilepsy Syndrome (FIRES) in the Acute and Chronic Phases. Journal of Child Neurology. 32: 35-40. PMID 27655472 DOI: 10.1177/0883073816669450  0.393
2016 Tomlinson SB, Bermudez C, Conley C, Brown MW, Porter BE, Marsh ED. Spatiotemporal Mapping of Interictal Spike Propagation: A Novel Methodology Applied to Pediatric Intracranial EEG Recordings. Frontiers in Neurology. 7: 229. PMID 28066315 DOI: 10.3389/Fneur.2016.00229  0.447
2016 Shen D, Hernandez CC, Shen W, Hu N, Poduri A, Shiedley B, Rotenberg A, Datta AN, Leiz S, Patzer S, Boor R, Ramsey K, Goldberg E, Helbig I, Ortiz-Gonzalez XR, ... ... Marsh ED, et al. De novo GABRG2 mutations associated with epileptic encephalopathies. Brain : a Journal of Neurology. PMID 27864268 DOI: 10.1093/Brain/Aww272  0.417
2016 Li D, Yuan H, Ortiz-Gonzalez XR, Marsh ED, Tian L, McCormick EM, Kosobucki GJ, Chen W, Schulien AJ, Chiavacci R, Tankovic A, Naase C, Brueckner F, von Stülpnagel-Steinbeis C, Hu C, et al. GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers. American Journal of Human Genetics. PMID 27616483 DOI: 10.1016/J.Ajhg.2016.07.013  0.407
2016 de Lange IM, Helbig KL, Weckhuysen S, Møller RS, Velinov M, Dolzhanskaya N, Marsh E, Helbig I, Devinsky O, Tang S, Mefford HC, Myers CT, van Paesschen W, Striano P, van Gassen K, et al. De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy. Journal of Medical Genetics. PMID 27358180 DOI: 10.1136/Jmedgenet-2016-103909  0.362
2016 Hazra A, Corbett BF, You JC, Aschmies S, Zhao L, Li K, Lepore AC, Marsh ED, Chin J. Corticothalamic network dysfunction and behavioral deficits in a mouse model of Alzheimer's disease. Neurobiology of Aging. 44: 96-107. PMID 27318137 DOI: 10.1016/J.Neurobiolaging.2016.04.016  0.361
2016 Devinsky O, Marsh E, Friedman D. Cannabidiol in patients with treatment-resistant epilepsy - Authors' reply. The Lancet. Neurology. 15: 545-6. PMID 27302119 DOI: 10.1016/S1474-4422(16)00120-4  0.345
2016 Marsh ED, Nasrallah MP, Walsh C, Murray KA, Nicole Sunnen C, McCoy A, Golden JA. Developmental interneuron subtype deficits after targeted loss of Arx. Bmc Neuroscience. 17: 35. PMID 27287386 DOI: 10.1186/S12868-016-0265-8  0.339
2015 Devinsky O, Marsh E, Friedman D, Thiele E, Laux L, Sullivan J, Miller I, Flamini R, Wilfong A, Filloux F, Wong M, Tilton N, Bruno P, Bluvstein J, Hedlund J, et al. Cannabidiol in patients with treatment-resistant epilepsy: an open-label interventional trial. The Lancet. Neurology. PMID 26724101 DOI: 10.1016/S1474-4422(15)00379-8  0.378
2015 Ng JM, Martinez D, Marsh ED, Zhang Z, Rappaport E, Santi M, Curran T. Generation of a mouse model of atypical teratoid/rhabdoid tumor of the central nervous system through combined deletion of Snf5 and p53. Cancer Research. PMID 26363008 DOI: 10.1158/0008-5472.Can-15-0874  0.301
2015 Skjei KL, Church EW, Harding BN, Santi M, Holland-Bouley KD, Clancy RR, Porter BE, Heuer GG, Marsh ED. Clinical and histopathological outcomes in patients with SCN1A mutations undergoing surgery for epilepsy. Journal of Neurosurgery. Pediatrics. 1-7. PMID 26339958 DOI: 10.3171/2015.5.Peds14551  0.417
2014 Pierson TM, Yuan H, Marsh ED, Fuentes-Fajardo K, Adams DR, Markello T, Golas G, Simeonov DR, Holloman C, Tankovic A, Karamchandani MM, Schreiber JM, Mullikin JC, Tifft CJ, et al. GRIN2A mutation and early-onset epileptic encephalopathy: personalized therapy with memantine. Annals of Clinical and Translational Neurology. 1: 190-198. PMID 24839611 DOI: 10.1002/Acn3.39  0.346
2014 Simonet JC, Sunnen CN, Wu J, Golden JA, Marsh ED. Conditional Loss of Arx From the Developing Dorsal Telencephalon Results in Behavioral Phenotypes Resembling Mild Human ARX Mutations. Cerebral Cortex (New York, N.Y. : 1991). PMID 24794919 DOI: 10.1093/Cercor/Bhu090  0.457
2014 Matalon D, Goldberg E, Medne L, Marsh ED. Confirming an expanded spectrum of SCN2A mutations: a case series. Epileptic Disorders : International Epilepsy Journal With Videotape. 16: 13-8. PMID 24659627 DOI: 10.1684/Epd.2014.0641  0.442
2014 Sunnen CN, Simonet JC, Marsh ED, Golden JA. Arx is required for specification of the zona incerta and reticular nucleus of the thalamus. Journal of Neuropathology and Experimental Neurology. 73: 253-61. PMID 24487799 DOI: 10.1097/Nen.0000000000000048  0.351
2013 Mirzaa GM, Paciorkowski AR, Marsh ED, Berry-Kravis EM, Medne L, Alkhateeb A, Grix A, Wirrell EC, Powell BR, Nickels KC, Burton B, Paras A, Kim K, Chung W, Dobyns WB, et al. CDKL5 and ARX mutations in males with early-onset epilepsy. Pediatric Neurology. 48: 367-77. PMID 23583054 DOI: 10.1016/J.Pediatrneurol.2012.12.030  0.374
2013 Ortiz-González XR, Poduri A, Roberts CM, Sullivan JE, Marsh ED, Porter BE. Focal cortical dysplasia is more common in boys than in girls. Epilepsy & Behavior : E&B. 27: 121-3. PMID 23416281 DOI: 10.1016/J.Yebeh.2012.12.035  0.383
2013 Paciorkowski AR, Traylor RN, Rosenfeld JA, Hoover JM, Harris CJ, Winter S, Lacassie Y, Bialer M, Lamb AN, Schultz RA, Berry-Kravis E, Porter BE, Falk M, Venkat A, Vanzo RJ, ... ... Marsh ED, et al. MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways. Neurogenetics. 14: 99-111. PMID 23389741 DOI: 10.1007/S10048-013-0356-Y  0.472
2013 Marsh ED. Fishing for the mechanisms causing febrile seizures: Employing a novel model to uncover the physiological generators of seizures with fever Experimental Neurology. 240: 108-111. PMID 23178581 DOI: 10.1016/J.Expneurol.2012.11.016  0.415
2012 Huang C, Marsh ED, Ziskind DM, Celix JM, Peltzer B, Brown MW, Storm PB, Litt B, Porter BE. Leaving tissue associated with infrequent intracranial EEG seizure onsets is compatible with post-operative seizure freedom. Journal of Pediatric Epilepsy. 1: 211-219. PMID 24563805 DOI: 10.3233/Pep-12033  0.419
2012 Wang IT, Allen M, Goffin D, Zhu X, Fairless AH, Brodkin ES, Siegel SJ, Marsh ED, Blendy JA, Zhou Z. Loss of CDKL5 disrupts kinome profile and event-related potentials leading to autistic-like phenotypes in mice. Proceedings of the National Academy of Sciences of the United States of America. 109: 21516-21. PMID 23236174 DOI: 10.1073/Pnas.1216988110  0.35
2012 Smart O, Maus D, Marsh E, Dlugos D, Litt B, Meador K. Mapping and mining interictal pathological gamma (30-100 Hz) oscillations with clinical intracranial EEG in patients with epilepsy. Expert Systems With Applications. 39: 7355-7370. PMID 23105174 DOI: 10.1016/J.Eswa.2012.01.071  0.45
2011 Gupta JR, Marsh ED, Nieh HA, Porter BE, Litt B. Discrete gamma oscillations identify the seizure onset zone in some pediatric epilepsy patients. Conference Proceedings : ... Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual Conference. 2011: 3095-8. PMID 22254994 DOI: 10.1109/IEMBS.2011.6090845  0.324
2011 Blanco JA, Stead M, Krieger A, Stacey W, Maus D, Marsh E, Viventi J, Lee KH, Marsh R, Litt B, Worrell GA. Data mining neocortical high-frequency oscillations in epilepsy and controls. Brain : a Journal of Neurology. 134: 2948-59. PMID 21903727 DOI: 10.1093/Brain/Awr212  0.397
2011 Paciorkowski AR, Thio LL, Rosenfeld JA, Gajecka M, Gurnett CA, Kulkarni S, Chung WK, Marsh ED, Gentile M, Reggin JD, Wheless JW, Balasubramanian S, Kumar R, Christian SL, Marini C, et al. Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function. European Journal of Human Genetics : Ejhg. 19: 1238-45. PMID 21694734 DOI: 10.1038/Ejhg.2011.121  0.375
2011 Abend NS, Gutierrez-Colina A, Zhao H, Guo R, Marsh E, Clancy RR, Dlugos DJ. Interobserver reproducibility of electroencephalogram interpretation in critically ill children. Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society. 28: 15-9. PMID 21221016 DOI: 10.1097/Wnp.0B013E3182051123  0.372
2010 Ahmad S, Marsh ED. Febrile Status Epilepticus: Current State of Clinical and Basic Research Seminars in Pediatric Neurology. 17: 150-154. PMID 20727483 DOI: 10.1016/J.Spen.2010.06.004  0.411
2010 Marsh ED, Peltzer B, Brown MW, Wusthoff C, Storm PB, Litt B, Porter BE. Interictal EEG spikes identify the region of electrographic seizure onset in some, but not all, pediatric epilepsy patients. Epilepsia. 51: 592-601. PMID 19780794 DOI: 10.1111/J.1528-1167.2009.02306.X  0.439
2010 Marsh ED, Golden JA. Aristaless-related homeobox mutations Epilepsia. 51: 70. DOI: 10.1111/J.1528-1167.2010.02856.X  0.453
2009 Marsh ED, Golden JA. Developing an animal model for infantile spasms: pathogenesis, problems and progress. Disease Models & Mechanisms. 2: 329-35. PMID 19553693 DOI: 10.1242/Dmm.001883  0.441
2009 Abend NS, Marsh E. Convulsive and nonconvulsive status epilepticus in children Current Treatment Options in Neurology. 11: 262-272. PMID 19523352 DOI: 10.1007/S11940-009-0030-8  0.356
2009 Marsh E, Fulp C, Gomez E, Nasrallah I, Minarcik J, Sudi J, Christian SL, Mancini G, Labosky P, Dobyns W, Brooks-Kayal A, Golden JA. Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females. Brain : a Journal of Neurology. 132: 1563-76. PMID 19439424 DOI: 10.1093/Brain/Awp107  0.473
2008 Fulp CT, Cho G, Marsh ED, Nasrallah IM, Labosky PA, Golden JA. Identification of Arx transcriptional targets in the developing basal forebrain. Human Molecular Genetics. 17: 3740-60. PMID 18799476 DOI: 10.1093/Hmg/Ddn271  0.401
2008 Marsh ED, Minarcik J, Campbell K, Brooks-Kayal AR, Golden JA. FACS-array gene expression analysis during early development of mouse telencephalic interneurons. Developmental Neurobiology. 68: 434-45. PMID 18172891 DOI: 10.1002/Dneu.20602  0.372
2007 Brown MW, Porter BE, Dlugos DJ, Keating J, Gardner AB, Storm PB, Marsh ED. Comparison of novel computer detectors and human performance for spike detection in intracranial EEG. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. 118: 1744-52. PMID 17544322 DOI: 10.1016/J.Clinph.2007.04.017  0.342
2007 Firpi H, Smart O, Worrell G, Marsh E, Dlugos D, Litt B. High-frequency oscillations detected in epileptic networks using swarmed neural-network features. Annals of Biomedical Engineering. 35: 1573-84. PMID 17541826 DOI: 10.1007/S10439-007-9333-7  0.398
2007 Gardner AB, Worrell GA, Marsh E, Dlugos D, Litt B. Human and automated detection of high-frequency oscillations in clinical intracranial EEG recordings. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. 118: 1134-43. PMID 17382583 DOI: 10.1016/J.Clinph.2006.12.019  0.301
2006 Marsh ED, Brooks-Kayal AR, Porter BE. Seizures and antiepileptic drugs: does exposure alter normal brain development? Epilepsia. 47: 1999-2010. PMID 17201696 DOI: 10.1111/J.1528-1167.2006.00894.X  0.399
2005 Marsh E, Melamed SE, Barron T, Clancy RR. Migrating partial seizures in infancy: Expanding the phenotype of a rare seizure syndrome Epilepsia. 46: 568-572. PMID 15816952 DOI: 10.1111/J.0013-9580.2005.34104.X  0.442
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